# Thoratec Corporation – FDA Inspection, Apr 3, 2017

Source: https://www.keypedia.com/records/fda_inspections/thoratec-corporation/f520c1d5-cd65-4402-8046-e381b78b6dfb
Source feed: FDA_Inspections

> FDA inspection 1006393 of Thoratec Corporation, April 03, 2017. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 812. Form 483 issued. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1006393
- Company Name: Thoratec Corporation
- Inspection Date: 2017-04-03
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 1054905 - 2018-05-17
- FDA Inspection 880973 - 2014-05-30
- FDA Inspection 772501 - 2012-03-16
- [FDA Inspection 629437 - 2009-10-13](https://www.keypedia.com/records/fda_inspections/thoratec-corporation/c59bcba4-5881-44c9-bf63-ff5d070ba357)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/kent-a-conforti/8d3d3e82-cd97-420e-8840-df92d6eeba09)

Company: https://www.keypedia.com/companies/thoratec-corporation/9895e06d-2699-4cd6-acfe-c45f50254a01

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7